HAPLOS Foundation

10/06/2026

LIVE | Kasaysayan at Kalayaan Tungo sa Paghubog Ng Kinabukasan

Sa pagdiriwang ng ika-128 (taon) Araw ng Kalayaan, balikan natin ang ating kasaysayan upang higit na maunawaan ang mga aral at mahahalagang pangyayaring humubog sa ating bayan.

Kilalanin natin ang naging mahalagang papel ni Apolinario Mabini—isang dakilang bayani at taong may kapansanan—sa pagtataguyod ng kalayaan, karapatan, at dignidad ng sambayanang Pilipino.

Live streaming at E-Net Philippines, PCUNCRPD, SeeSaw, NORFIL Foundation and other FB pages.

REPLAYS Available on InkluNasyon YouTube channel: https://youtube.com/

06/06/2026

🇵🇭 FROM GLOBAL ADVOCACY TO LOCAL ACTION

The recently adopted World Health Assembly Resolution on Hemophilia and Other Bleeding Disorders is more than a global milestone—it is a reminder that every person deserves access to timely diagnosis, comprehensive care, and effective treatment.

For the Philippines, it strengthens ongoing efforts to improve care for persons with bleeding disorders, including the development of a PhilHealth Hemophilia Treatment Package and continued advocacy for better access to treatment and support services.

Together, we move from global commitment to local action.

💚 Better Care • Better Access • Stronger Hope

03/06/2026

03/06/2026

📍HAPLOS COMMUNITY FAMILY DAY 2026
🗓️ May 31, 2026
📌 Town and Country Executive Village Clubhouse, Antipolo City

💚Tibay ng Pamilya, Lakas ng Bawat Isa💚

What a wonderful day of faith, friendship, learning, laughter, and shared experiences!

From our Holy Mass, family testimonies, psychosocial activities, WFH Congress reflections, games, raffles, dancing, singing, and fellowship, Family Day reminded us of the strength of our community and the importance of supporting one another through every challenge and every triumph.

This year's theme, "Tibay ng Pamilya, Lakas ng Bawat Isa," came to life through the stories, artwork, talents, and experiences shared by our members and families throughout the day.

Our heartfelt thanks to all participants, volunteers, sponsors, donors, healthcare professionals, and friends who helped make this gathering meaningful and memorable.

Together, we are stronger. Together, we are family. 💚

01/06/2026

🌍 One Global Community. One Shared Voice.

HAPLOS Foundation is honored to stand alongside more than 100 organizations worldwide in supporting the WFH Global Call to Action.

💚 Together, our voices create change.

24/05/2026

🌍 HISTORIC WORLD HEALTH ASSEMBLY RESOLUTION ADOPTED FOR HEMOPHILIA AND OTHER BLEEDING DISORDERS

The World Federation of Hemophilia (WFH) announced that the 79th World Health Assembly has officially adopted a landmark resolution on “Global Action to Advance Health Equity for People with Hemophilia and Other Bleeding Disorders.”

Led by Armenia as the proponent country and supported by WHO Member States, the resolution marks a historic step toward improving diagnosis, treatment access, comprehensive care, and health equity for persons living with bleeding disorders worldwide.

As the recognized National Member Organization of the WFH in the Philippines, HAPLOS Foundation joins the global bleeding disorders community in celebrating this important achievement and reaffirming our commitment to advancing better care, better access, and stronger support systems for Filipino persons with bleeding disorders and their families.

📄 Read the official WFH announcement here:
https://wfh.org/article/79th-world-health-assembly-adopts-historic-resolution-on-hemophilia-and-other-bleeding-disorders/

23/05/2026

Voices of Hope: The Hemophilia Community Speaks

As part of the continuing development of the PhilHealth Hemophilia Treatment Package, persons with hemophilia and families from different regions of the country recently participated in a Focus Group Discussion organized by PhilHealth to share their experiences, challenges, and hopes for better access to care.

In this video, Mr. Randolf Apanay, a person with Hemophilia A, shares his reflections and aspirations for a PhilHealth program that truly responds to the needs of persons with bleeding disorders.

Every voice shared brings us one step closer to better hemophilia care for all. 💚

20/05/2026

A HAPLOS Community Milestone!

🎉 Congratulations to Manuel Luis II “Louie” Turingan Sanchez for successfully passing the September 2025 Bar Examinations! ⚖️💚

Your HAPLOS Community family proudly celebrates this remarkable milestone and the perseverance, courage, and determination behind your success.

As a person with hemophilia, your journey is an inspiration to many — proving that challenges do not define limits, but can become sources of strength, purpose, and achievement.

May this accomplishment open even greater opportunities for you to serve, inspire, and make a difference in the lives of others.

We are proud of you, Attorney Louie! 💚⚖️

20/05/2026

💚 One family. One community. Stronger together. 💚

Join us as we celebrate the HAPLOS Community Family Day Gathering 2026 with the theme:

✨ “Tibay ng Pamilya, Lakas ng Bawat Isa” ✨

A day of fellowship, fun, healing, gratitude, and togetherness awaits our HAPLOS families through meaningful activities, games, psychosocial support, worship, music, and community bonding.

📅 May 31, 2026
🕗 8:00 AM – 3:30 PM
📍 Town & Country Executive Village Clubhouse, Antipolo City

Let us celebrate the strength of every person with hemophilia, every caregiver, and every family who continues to journey with courage and hope. 💙💚

17/05/2026

HEMOPHILIA AWARENESS LAY FORUM SERIES
SESSION 3: LIVING FULLY AND GETTING THE RIGHT HELP

💚 HAPLOS Community Successfully Concluded Session 3 of the Virtual Hemophilia Lay Forum! 💚

✨ Highlights:

🧠 Mr. Jun Angelo Sunglao, Psychologist, discussed coping with a lifelong condition and the importance of mental wellness.

🏥 Dr. Mara Louella Sangilan-Carpio, Hematology-Oncology Fellow of the National Children's Hospital, shared guidance on accessing proper care, support systems, and community resources.

🎤 Opening remarks were given by Ms. Herminia C. Palacio, moderated by Ms. Celsa P. Uy, with closing remarks from Mr. Reynaldo Sarmenta.

This final session reminded us that living with hemophilia is not only about treatment—but also about resilience, support, and community.

Thank you to all who joined us in this meaningful educational series. Together, we continue building a stronger and more empowered hemophilia community. 💚